Correlation between SD-OCT, immunocytochemistry and functional findings in an animal model of retinal degeneration

Purpose: The P23H rhodopsin mutation is an autosomal dominant cause of retinitis pigmentosa (RP). The degeneration can be tracked using different anatomical and functional methods. In our case, we evaluated the anatomical changes using Spectral-Domain Optical Coherence Tomography (SD-OCT) and correl...

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Detalles Bibliográficos
Autores principales: Cuenca, Nicolás, Fernández-Sánchez, Laura, Sauvé, Yves, Segura, Francisco J., Martínez-Navarrete, Gema, Tamarit, José Manuel, Fuentes-Broto, Lorena, Sanchez-Cano, Ana, Pinilla, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273614/
https://www.ncbi.nlm.nih.gov/pubmed/25565976
http://dx.doi.org/10.3389/fnana.2014.00151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273614/
https://www.ncbi.nlm.nih.gov/pubmed/25565976
http://dx.doi.org/10.3389/fnana.2014.00151

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